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Guide - ANVISA Registration 81325990101

Access comprehensive regulatory information for Guide in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81325990101 and manufactured by BIOMETRIX LTD. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including DPS INDUSTRIA, DISTRIBUICAO, COMERCIO, IMPORTACAO E EXPORTACAO LTDA, CPMH - Comércio e Indústria de Produtos Médico-Hospitalares e Odontológicos LTDA., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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81325990101
Registration Details
ANVISA Registration Number: 81325990101
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Device Details

Fio Guia para Angiografia Biometrix
Risk Class II

Registration Details

81325990101

25351202600201970

19933144000129

Company Information

BIOMETRIX LTD
Israel
PT: ISRAEL

Dates and Status

Sep 16, 2019

VIGENTE

09/18/2025 19:00:01